Table I.
No.a | Name | Age Estimatesf | n | C3 Sister Group | C4 Subtype(s) | Cropsm | Habitatn |
---|---|---|---|---|---|---|---|
1b | Stipagrostis | 15.1 (±4.6)–7.5 (±3.1) | 50 | Sartidiaa | NADP-ME | – | Deserts and semideserts |
NA | |||||||
2b | Aristida | 28.8 (±5.2)–14.4 (±4.7) | 290 | Sartidiaa | NADP-ME | – | Large ecological range |
[44.4 (±7.5)–present] | |||||||
3b | Core Chloridoideae | 32.0 (±4.4)–25.0 (±4.0) | 1,410 | Merxmuellera rangeiag | NAD-ME and PCK | Finger millet, teff | Large ecological range |
[37.6 (±6.6)–22.5 (±5.7)] | |||||||
4b | Centropodia | 22.0 (±4.6)–11.3 (±5.5) | 4 | M. rangeiag | NAD-ME | – | Dry open habitats (semideserts) |
NA | |||||||
5c | Eriachne | 11.5 (±3.6)–6.6 (±2.8) | 40 | Isachneagh | NADP-ME | – | Warm open habitats (savannah) |
NA | |||||||
6b | Arundinelleae | 26.4 (±4.4)–7.9 (±3.4) | 95 | Centotheceae 2agh | NADP-ME | – | Large ecological range |
[31.7 (±5.9)–present] | |||||||
7cd | Panicum/Urochloa/Setaria clade | 18.5 (±3.7)–16.4 (±3.6) | >530 | C3Neurachnea | NADP-ME, NAD-ME, and PCK | Foxtail, pearl, and proso millets | Large ecological range |
[15.9 (±3.7)–13.1 (±3.2)] | |||||||
8c | Neurachne munroi | 4.4 (±3.3)–present | 1 | Neurachne tenuifoliaa | NADP-ME | – | Dry open habitats (steppes) |
NA | |||||||
9c | Echinochloa | 13.8 (±3.5)–4.4 (±2.8) | 30–40 | Parodiophyllochloaai | NADP-ME | – | Warm open habitats |
[20.6 (±4.5)–2.6 (±1.3)] | |||||||
10b | Alloteropsis | 15.3 (±3.5)–present | 4–7 | Forest shade cladeaj | NADP-ME and PCK | – | Warm open habitats (savannah) |
NA | |||||||
11cd | Digitaria | 21.2 (±3.9)–8.1 (±3.4) | 220 | x = 9 Paniceaea | NADP-ME | Fonio | Various warm open habitats |
[15.9 (±3.7)–5.4 (±2)] | |||||||
12b | Andropogoneae | 21.9 (±3.9)–17.1 (±4.1) | 1,085 | x = 10 Paniceaeak | NADP-ME | Maize, sorghum, sugarcane | Large ecological range |
[24.3 (±4.9)–19.1 (±4.5)] | |||||||
13ab | Paspalum clade | 14.1 (±3.4)–8.5 (±3.1) | >345 | Streptostachys asperifoliaak | NADP-ME | Kodo millet | Warm open habitats (savannah) |
[11.7 (±3.1)–present] | |||||||
13bc | Ophiochloa clade | 10.6 (±3.3)–2.8 (±1.9) | 115 | S. asperifoliaa | NADP-ME | – | Large ecological range |
[13.7 (±3.5)–4.4 (±2.1)] | |||||||
14b | Anthaenantiae | 14.3 (±3.5)–present | 1 | Steinchisma cladeak | NADP-ME | – | Warm open habitats (savannah) |
[15 (±3.7)–present] | |||||||
15c | Streptostachys ramosa | 15.5 (±3.5)–present | 1 | Cyphonanthusl | NADP-ME | – | Warm open habitats (savannah) |
[16.3 (±3.7)–present] | |||||||
16b | Panicum prionitis clade | 10.4 (±2.9)–6.3 (±2.7) | >5 | Arthropogon lanceolatusak | NADP-ME | – | Warm open habitats (savannah) |
[11.2 (±2.9)–present] | |||||||
17c | Mesosetum clade | 12.3 (±3.2)–11.3 (±3.0) | 40 | Homolepisak | NADP-ME | Warm open habitats (savannah) | |
[14.8 (±3.5)–13.9 (±3.4)] |
Independent origin confirmed by PEPC analyses (Christin et al., 2007).
Independent origin based on putative species relationships only.
Phylogeny from Vicentini et al. (2008) found Digitaria and the main x = 9 Paniceae C4 clade clustered together, suggesting a single C4 origin.
Previously named Leptocoryphium lanatum.
Christin et al. (2008) and Vicentini et al. (2008) into square brackets, ages are given in millions of years.
C3 subspecies of A. semialata could represent a reversion from C4 to C3 (Ibrahim et al., 2009).
Excluding fodders.